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rs2952615

From SNPedia

Orientationminus
Make rs2952615(C;C)
Make rs2952615(C;G)
Make rs2952615(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position112803191
GeneAPC
is asnp
is mentioned by
dbSNPrs2952615
ebirs2952615
HLIrs2952615
Exacrs2952615
Varsomers2952615
Maprs2952615
PheGenIrs2952615
hapmaprs2952615
1000 genomesrs2952615
hgdprs2952615
ensemblrs2952615
gopubmedrs2952615
geneviewrs2952615
scholarrs2952615
googlers2952615
pharmgkbrs2952615
gwascentralrs2952615
openSNPrs2952615
23andMers2952615
23andMe allrs2952615
SNP Nexus

SNPshotrs2952615
SNPdbers2952615
MSV3drs2952615
GWAS Ctlgrs2952615
Max Magnitude
? (C;C) (C;G) (G;G) 28
ClinVar
Risk rs2952615(G;G)
Alt rs2952615(G;G)
Reference rs2952615(C;C)
Significance Other
Disease Familial colorectal cancer
Variation info
Gene APC
CLNDBN Familial colorectal cancer
Reversed 1
HGVS NC_000005.9:g.112138888G>C
CLNSRC
CLNACC RCV000074036.1,